Tag | Content |
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EnhancerAtlas ID | HS101-40486 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:76633620-76634860 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr7:76634827-76634848 | TTCTCCCCTCCCACCTCCATC | - | 6.18 | ZNF263 | MA0528.1 | chr7:76634824-76634845 | GCTTTCTCCCCTCCCACCTCC | - | 6.22 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_24154 | chr7:76633438-76636379 | Colon_Crypt_2 | SE_26739 | chr7:76630193-76636864 | Esophagus | SE_68923 | chr7:76631414-76636453 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I077000 | chr7 | 76630194 | 76636864 |
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Enhancer Sequence | CAAGGTGAGT GCCACCATGC GCCCCGGGGG TGGACGGGGC CCTGACCAGG CGGCAGGAGG 60 CCAGGCGCCA CACTGGACTC TGTTTCTGCA GCGGAGGACA GAGGCTGAGG CCGGGCCGAG 120 TGTCTGCTGC TCTTTTCTGG GGACCTGCTG TAGGTACAGG GAGGGCAGCC TGGACCTCAC 180 ATAGCCTCGA GGGAGGAGGA GAGGCCATCA CCTTCCAGCA CCCTGCCGGG TGGGGTCAGG 240 AGCTCCTGAG AGTTAGAGTG TGACAGGCAG GGACCGGGGG CTGTGTTAGA CCAGGTGACC 300 ACGGAAGGCT GGAGCAGTGG TGTCTGCACT GTGACATGAA TAGGGACTTT GTGGCTGCAG 360 CCAGACCCAA GGGGCTGGGG GCCCTGCTGG AGTGATTGGA CCCTGGGCGC CCACCCCCCT 420 CCGATTGGGA GAGGCAGCCC CAGGGACCCC CACGCCTGTC TCCGTGGCTC ACCTTTTGTC 480 CCCCGTGGCC ACAGAGCTGG TGCCCTACAC ACCACAGATA ACAGCTTGGG ACCTGGAAGG 540 GAAGGTCACA GCCACCACCT TCTCCCTGGA GCAGCCGCGC TGTGTCTTCG ATGGGCTTGC 600 CAGCGCCAGC GATACCGTCT GGCTCGTGGT GGCCTTCAGC AATGGTGCGG GGACTGCTGT 660 GGGGCCTGGG TGAGGGTGAC GGCTGAGGAG AGTGGTGGGC CCTAGGAGCC CCTCACCAGC 720 AAGCGCCTTC AATGATTGAG CCCCTGTGGG GGCCTTTGGG AGAGTAGGTG TGGATGAATT 780 GGGCTTTATC TAAAGGGGTA ATATGTGTAT TGAAAAATAC ACACGTAGTG AACACCAAAT 840 CCTGGGAGTA GTGCAAGTGG TGGGTTTGTC AGCTGTCAAG GGCTCTGCAA CCCTTTCTCT 900 GAATCCAAGT AGTTCTTCCT TTGGACAGGG AACCGAGGCT GCGACCTGGG AGGATGTGGC 960 CTCCTGTGGG GCAGGGCCGG TGCACTGCGA TGGGGCTGGG GCTGGCGCTG GGCAGGTTGG 1020 GACTGCCCGC TGCTCCCCAC TCCTGGCTCT GGGTGGGGAC AAAAGGCCAG AGGGAAGCTC 1080 CCCTTCAGGG GTAACAAAGT CGACTGGGTC TGGACTATCT CTGGGGGCCC TGAGGGAGGA 1140 GGTGGCATGG GGGGTCAGGG CTGGAGACTG GGCGAACACA GAACCCCCTC ATAAGGACAA 1200 AGCTGCTTTC TCCCCTCCCA CCTCCATCTG TTCTCTCCTC 1240
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